Canonical Allele Identifier: CA1428762797
Gene: CLDN16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408420T= , CM000665.2:g.190408420T= GRCh38
NC_000003.11:g.190126209T= , CM000665.1:g.190126209T= GRCh37
NC_000003.10:g.191608903T= NCBI36
NG_008149.1:g.25369T=

Transcript Alleles

HGVS Amino-acid change
ENST00000264734.3:c.489T= MANE Select ENSP00000264734.3:p.Gly163=
ENST00000456423.2:c.115-1483T= ENSP00000414136.2:n.115-1483T=
ENST00000264734.2:c.699T= ENSP00000264734.2:p.Gly233=
ENST00000456423.1:c.325-1483T= ENSP00000414136.1:n.325-1483T=
NM_006580.3:c.699T= NP_006571.1:p.Gly233=
NM_001378492.1:c.489T= NP_001365421.1:p.Gly163=
NM_001378493.1:c.489T= NP_001365422.1:p.Gly163=
NM_006580.4:c.489T= MANE Select NP_006571.2:p.Gly163=